HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650125Generated: November 1, 2026
Hydrochloric Acid → 6-Chloro-1-methyl-3-n-octyl-uracil
https://huagongshe.com/reaction/1650125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Uracil, 6-chloro-1-methyl- | HCID 3015589 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-1-methyl-3-n-octyl-uracil | HCID 23053624 | — |
Reaction Steps
Next 5.4 ml of n-octyl bromide was added to a solution consisting of 5 grams of 6-chloro-1-methyl-uracil obtained as described above, 5.2 grams of potassium carbonate and 50 ml of N,N-dimethylformamide and the mixture was heated to 90° C. and stirred for a period of 5 hours. After cooling, the reaction mixture was added slowly to a solution of 10 ml of concentrated hydrochloric acid and 300 ml of water. The resulting solution was extracted twice with 100 ml of chloroform and, after drying over magnesium sulfate, the chloroform layer was concentrated under reduced pressure. The concentrate was then refined using silica gel column chromatography, whereupon 3.1 grams of 6-chloro-1-methyl-3-n-octyl-uracil was obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923789 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-d2e62a0e53d043f4972f5250144a878a |
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| Source note | uspto-grants-1990_05 |
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